Pharma company: renaudin laboratoire

List of renaudin laboratoire products:

• Adrenaline
• Aminophylline - SPL UNCLASSIFIED SECTION Aminophylline Injection, USP 25 mg/mL Aminophylline, Dihydrate (Equivalent to 19.7 mg/mL of Anhydrous Theophylline) ...
• Atropine - An alkaloid, originally from Atropa belladonna, but found in other plants, mainly solanaceae. [PubChem] Indication: For the treatment of poisoning by susceptible organophosphorous nerve agents having cholinesterase activity as well as organophosphorous or carbamate insecticides. Atropine, a naturally occurring belladonna alkaloid, is a racemic mixture of equal parts of d- and l-hyoscyamine, whose activity is due almost entirely to the levo isomer of the drug. Atropine is commonly classified as...
• Bicarbonate de Sodium
• Chlorhydrate de Metoclopramide
• Chlorure de Potassium
• Chlorure de Sodium - Pharmacological action Ions of sodium and chlorine are the major inorganic components of the extracellular fluid, maintaining an appropriate osmotic pressure of blood plasma and extracellular fluid. Isotonic solution of Sodium Chloride fills a deficit of body fluids during dehydration. Hypertonic solution of sodium chloride for IV injection provides a correction of osmotic pressure of extracellular fluid and blood plasma. When applied topically in ophthalmology sodium chloride has...
• Cyanocobalamine
• Diazepam - SPL UNCLASSIFIED SECTION Fliptop Vial Rx only CIV WARNING: RISKS FROM CONCOMITANT USE WITH OPIOIDS Concomitant use of benzodiazepines and opioids may result in profound sedation, respiratory depression, coma, and death...
• Diclofenac - Pharmacological action NSAIDs, a derivative of phenylacetic acid, diclofenac has a pronounced anti-inflammatory, analgesic and mild antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to two mechanisms: peripheral (indirectly, through suppression of prostaglandin...
• Dopamine - One of the catecholamine neurotransmitters in the brain. It is derived from tyrosine and is the precursor to norepinephrine and epinephrine. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement. A family of receptors (receptors, dopamine) mediate its action. [PubChem] Indication: For the correction of hemodynamic imbalances present in the shock syndrome due to myocardial infarction, trauma, endotoxic septicemia, open-heart surgery,...
• Ephedrine - An alpha- and beta-adrenergic agonist that may also enhance release of norepinephrine. It has been used in the treatment of several disorders including asthma, heart failure, rhinitis, and urinary incontinence, and for its central nervous system stimulatory effects in the treatment of narcolepsy and depression. It has become less extensively used with the advent of more selective agonists. [PubChem] Indication: Ephedrine commonly used as a stimulant, appetite suppressant, concentration aid,...
• Fentanyl - SPL UNCLASSIFIED SECTION For Topical Application in Dogs Only Opioid Analgesic NOT FOR INJECTION 50 mg/mL (500 mg/10 mL) CAUTION: Federal law restricts this drug to use by or on the order of a licensed...
• Furosemide - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
• Glucalcium
• Glucose
• Haloperidol - WARNING Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7...
• Hydroxyzine - Hydroxyzine information This medication is made by Pfizer and is generically known as hydroxyzine hydrochloride and is available in tablet and syrup form. Hydroxyzine indications This drug is prescribed for the relief of anxiety and tension brought about by psychoneurosis. Hydroxyzine may also be used for the containment of pruritus due to allergic reactions such as chronic uticaria and contact dermatitis. Hydroxyzine may be used as a sedative when used as a premedication following...
• Lidocaine - Pharmacological action Lidocaine is an antiarrhythmic agent of class IB, local anesthetic, a derivative of acetanilide. This medication has membrane stabilizing activity. Lidocaine causes a blockade of sodium channels of excitable membranes of neurons and the membrane of cardiomyocytes. This drug reduces the duration of the action potential and effective refractory period in Purkinje fibers, inhibits their automaticity. In this case, lidocaine inhibits electrical activity in depolarized,...
• Magnesium Sulfate - SPL UNCLASSIFIED SECTION Magnesium Sulfate Injection, USP Ansyr™ Plastic Syringe Rx...
• Morphine - DESCRIPTION Opium Tincture, USP (Deodorized), is for oral administration. It is freed from unpleasant odor or nauseating substances by “denarcotization” with a petroleum distillate. Opium tincture is a clear, reddish-brown hydroalcoholic solution. Each 100 mL contains 1 g of anhydrous morphine (represents the equivalent of 10 g of Powdered Opium, USP), alcohol, 19%, and water. Opium has a very characteristic odor and...
• Nalbuphine - A narcotic used as a pain medication. It appears to be an agonist at kappa opioid receptors and an antagonist or partial agonist at mu opioid receptors. [PubChem] Indication: For the relief of moderate to severe pain. Nalbuphine is a synthetic opioid agonist-antagonist analgesic of the phenanthrene series. Nalbuphine's analgesic potency is essentially equivalent to that of morphine on a milligram basis. The opioid antagonist activity of nalbuphine is one-fourth as potent as nalorphine and 10...
• Noradrenaline
• Noradrenaline Sans Conservateur
• Ondansetron - Warnings and Precautions, ( 5.3 ) 09/2014 1 INDICATIONS AND USAGE ZUPLENZ is a 5-HT3 receptor antagonist indicated for: ...
• Papaverine - An alkaloid found in opium but not closely related to the other opium alkaloids in its structure or pharmacological actions. It is a direct-acting smooth muscle relaxant used in the treatment of impotence and as a vasodilator, especially for cerebral vasodilation. The mechanism of its pharmacological actions is not clear, but it apparently can inhibit phosphodiesterases and it may have direct actions on calcium channels. [PubChem] Indication: For the treatment of impotence and vasospasms....
• Pethidine
• Phosphate Monopotassique
• Pyridoxine - Pyridoxine is the 4-methanol form of vitamin B6 and is converted to pyridoxal 5-phosphate in the body. Pyridoxal 5-phosphate is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and vitamin B6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading. [PubChem] Indication: For the treatment of vitamin B6 deficiency and for the...
• Salbutamol - Salbutamol is a short-acting, selective beta2-adrenergic receptor agonist used in the treatment of asthma and COPD. It is 29 times more selective for beta2 receptors than beta1 receptors giving it higher specificity for pulmonary beta receptors versus beta1-adrenergic receptors located in the heart. Salbutamol is formulated as a racemic mixture of the R- and S-isomers. The R-isomer has 150 times greater affinity for the beta2-receptor than the S-isomer and the S-isomer has been associated with...
• Scopolamine - An alkaloid from Solanaceae, especially Datura metel L. and Scopola carniolica. Scopolamine and its quaternary derivatives act as antimuscarinics like atropine, but may have more central nervous system effects. Among the many uses are as an anesthetic premedication, in urinary incontinence, in motion sickness, as an antispasmodic, and as a mydriatic and cycloplegic. [PubChem] Indication: For the treatment of excessive salivation, colicky abdominal pain, bradycardia, sialorrhoea, diverticulitis,...
• Sodium Bicarbonate - Enter section text here Active ingredient                                           Purpose (in each tablet) Sodium bicarbonate 10 gr (650 mg) .......      Antacid Enter section text...
• Sodium Chlorure - Pharmacological action Ions of sodium and chlorine are the major inorganic components of the extracellular fluid, maintaining an appropriate osmotic pressure of blood plasma and extracellular fluid. Isotonic solution of Sodium Chloride fills a deficit of body fluids during dehydration. Hypertonic solution of sodium chloride for IV injection provides a correction of osmotic pressure of extracellular fluid and blood plasma. When applied topically in ophthalmology sodium chloride has...
• Sufentanil - An opioid analgesic that is used as an adjunct in anesthesia, in balanced anesthesia, and as a primary anesthetic agent. [PubChem] Indication: Used as an analgesic adjunct in anesthesia and as a primary anesthetic drug in procedures requiring assisted ventilation and in the relief of pain. Sufentanil is a synthetic opioid analgesic. Sufentanil interacts predominately with the opioid mu-receptor. These mu-binding sites are discretely distributed in the human brain, spinal cord, and other tissues...

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The information was verified by Dr. Rachana Salvi, MD Pharmacology